Hereditary Hyperferritinemia-Cataract Syndrome: Two Novel Mutations in the L-Ferritin Iron-Responsive Element
- 1 January 1998
- journal article
- Published by American Society of Hematology in Blood
- Vol. 91 (1) , 367-368
- https://doi.org/10.1182/blood.v91.1.367
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Hereditary Hyperferritinemia-Cataract Syndrome: Relationship Between Phenotypes and Specific Mutations in the Iron-Responsive Element of Ferritin Light-Chain mRNABlood, 1997
- The interaction between the iron-responsive element binding protein and its cognate RNA is highly dependent upon both RNA sequence and structureNucleic Acids Research, 1993
- Mutagenesis of the iron-regulatory element further defines a role for RNA secondary structure in the regulation of ferritin and transferrin receptor expression.Journal of Biological Chemistry, 1992
- Structural requirements of iron-responsive elements for binding of the protein involved in both transferrin receptor and ferritin mRNA post-transcriptional regulationNucleic Acids Research, 1990